-
- Posts: 25
- Joined: Wed Aug 01, 2007 10:23 am
I need some advice on acidifying samples. They are all prepared from different biological matrices, some containing a lot proteins/peptides and some less. The compounds I am interested in are pretty nonpolar (steroids).
My setup consists of Oasis HLB in an online cleanup setup coupled with an analytical column and MS/MS.
I have been adviced to acidify my samples. As far I understand this has two effects:
1. Put protein/peptides in a uniformly charged states so that they interfere less with the HLB column.
2. Disrupt any protein binding of my steroids from proteins.
This may give a cleaner signal, decrease ionsuppression and increase recovery.
My question is simple. How strong should this acid be? And how much should I add? (What pH is needed?)
Is 2% Formic acid enough? (that would simplify things for me...)
